JuggerLocRecalls & reported problems across all models

We found 2 models of JuggerLoc by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

2 FDA recall records name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

JuggerLoc recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Oct 21, 2024Class IIOpen, Classified

   Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to surgical intervention.

   Z-0477-2025 · Root cause: Process control · Recall details · FDA record ↗

2. Feb 14, 2022Class IITerminated

   Packaging of various implants may not have sufficient adhesion on all sides, leading to loss of sterile barrier integrity. Use of product poses risk of infection, leading to surgical intervention, and/or extension of surgery to find another part.

   Z-0809-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

JuggerLoc models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• JuggerLoc™ 110027357

  Kit, surgical instrument, disposable
  1 recall0 reports
• JuggerLoc™ 110010371

  Staple, fixation, bone
  1 recall0 reports

Other Biomet Orthopedics, LLC products

• AFFIXUSHIP FRACTURE NAIL - RIGHT39 models · 6 reports · 37 recalls
• AFFIXUSHIP FRACTURE NAIL - LEFT27 models · 7 reports · 24 recalls
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• Arcos Modular Revision Hip System71 models · 191 reports · 19 recalls
• Comprehensive Reverse Shoulder57 models · 895 reports · 3 recalls
• Vanguard Knee System147 models · 306 reports · 13 recalls
• STAGEONE17 models · 0 reports · 18 recalls
• StageOne Select15 models · 2 reports · 15 recalls